Примери за използване на Referred to in this regulation на Английски и техните преводи на Български
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Colloquial
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Medicine
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Ecclesiastic
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Ecclesiastic
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The following authorities shall be involved in the authorisation and supervision of CSDs where specifically referred to in this Regulation.
Category A: technical services which carry out in their own facilities the tests referred to in this Regulation and in the acts listed in Annex I;
The delegations of power referred to in this Regulation shall be conferred for an indeterminate period of time from the date of entry into force of this Regulation. .
Member States shall establish reporting systems for the relevant sectors referred to in this Regulation, with the objective of acquiring, to the extent possible, emission data.
(b) category B: supervising the tests referred to in this Regulation, where such tests are performed in the facilities of a manufacturer or of a third party;
as well as the academic community, beyond those referred to in this Regulation.
The autonomous Common Customs Tariff duties for the products referred to in this regulation are partially
Dioxins as referred to in this Regulation cover a group of 75 polychlorinated dibenzo-p-dioxin(PCDD)
implementing standards as well as the guidelines and recommendations referred to in this Regulation.'.
operational control of the activities referred to in this Regulation are exercised;
(4) The information referred to in this Regulation shall be kept for a minimum of 3 years after the death
in the production, maintenance or servicing, including the refilling, of products and equipment, or">in other processes referred to in this Regulation".
operational control of the activities referred to in this Regulation are exercised;
groups of such persons whose professional activities are the subject of the checks referred to in this Regulation shall not obstruct such checks
(b) category B: supervision of the tests referred to in this Regulation and in the acts listed in Annex IV,
including test preparation, referred to in this Regulation and in the acts listed in Annex IV,
which includes test preparation, referred to in this Regulation and in the regulatory acts listed in Annex II,
Member States shall be encouraged to apply the common procedural rules and methodology referred to in this Regulation for the clinical assessment of medicinal products
The competent national authorities shall grant them the powers referred to in this Regulation in order to be able to fulfil their tasks.
the ability to fulfil the tasks referred to in this Regulation, in particular those referred to in Article 79.